Evidence map›Paper›PMID 42219400›Full record

ArticleFunctional & integrative genomics2026

Transgene-free plant genome editing via viral delivery of miniature CRISPR-Cas12f.

Muhammad Jawad Akbar Awan, Afzal Akram, Rubab Zahra Naqvi, Mariam Akhtar, Saqib Siddique, Muhammad Ismail Buzdar, Imran Amin, Shahid Mansoor

Abstract read
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In one paragraph

Article in Functional & integrative genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Muhammad Jawad Akbar AwanAgricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Constituent College of Pakistan Institute of Engineering and Applied Sciences, Jhang Road, Faisalabad, Pakistan.ORCID http://orcid.org/0000-0001-6163-7740
Afzal AkramAgricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Constituent College of Pakistan Institute of Engineering and Applied Sciences, Jhang Road, Faisalabad, Pakistan.
Rubab Zahra NaqviAgricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Constituent College of Pakistan Institute of Engineering and Applied Sciences, Jhang Road, Faisalabad, Pakistan.
Mariam AkhtarAgricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Constituent College of Pakistan Institute of Engineering and Applied Sciences, Jhang Road, Faisalabad, Pakistan.
Saqib SiddiqueAgricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Constituent College of Pakistan Institute of Engineering and Applied Sciences, Jhang Road, Faisalabad, Pakistan.
Muhammad Ismail BuzdarAgricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Constituent College of Pakistan Institute of Engineering and Applied Sciences, Jhang Road, Faisalabad, Pakistan.
Imran AminAgricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Constituent College of Pakistan Institute of Engineering and Applied Sciences, Jhang Road, Faisalabad, Pakistan.
Shahid MansoorAgricultural Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Constituent College of Pakistan Institute of Engineering and Applied Sciences, Jhang Road, Faisalabad, Pakistan. shahidmansoor7@gmail.com.ORCID http://orcid.org/0000-0001-7418-1826

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Efficient delivery of CRISPR reagents into plant cells remains a major bottleneck, particularly for transgene-free genome editing. RNA viral vectors such as Tabacco Rattle Virus (TRV) provide an attractive platform for transient expression but are limited by their small cargo capacity. Recently discovered miniature nucleases like Cas12f, due to their compact size and high activity, offer a promising alternative for viral delivery systems. In this study, a plant codon-optimized Acidibacillus sulfuoxidans Cas12f (AsCas12f), fused with nuclear localization signals, was cloned into the TRV genome to develop a viral vector-based delivery platform. Two sgRNAs targeting the Nicotiana benthamiana PHYTOENE DESATURASE (NbPDS) gene were delivered through Agrobacterium-mediated infiltration. To enhance mobility and transcript abundance, mobile RNA elements such as modified Flowering Locus T (mFT), truncated FLOWERING LOCUS T (tFT), and transfer RNA of methionine (tRNA

Indexed as

CRISPR-Associated ProteinsCRISPR-Cas SystemsGene EditingGenome, PlantNicotianaGenetic VectorsOxidoreductasesPlants, Genetically ModifiedPlant VirusesTransgenesCRISPR-Associated ProteinsOxidoreductasesphytoene dehydrogenaseCRISPR-Cas12fFlowering locus TMobile RNANicotiana benthamianaNon-transgenicRNA-dependent RNA polymeraseTRVViral vector

Identifiers

PMID42219400

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.